(Q34401694)

1 August 2017

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders (English)

1 reference

1 August 2017

Eric M Morrow

5

0 references

Shafali S Jeste

Shafali S Jeste

4

0 references

Gerard Berry

Gerard T Berry

13

0 references

James F. Gusella

17

James F Gusella

1 reference

1 August 2017

29

Christopher A Walsh

1 reference

1 August 2017

22

David T Miller

1 reference

1 August 2017

25

Leonard Rappaport

1 reference

Children's Hospital Boston Genotype Phenotype Study Group

1 August 2017

34

Children's Hospital Boston Genotype Phenotype Study Group

1 reference

1 August 2017

Michael S L Ching

1

1 reference

1 August 2017

Yiping Shen

2

1 reference

1 August 2017

Wen-Hann Tan

3

1 reference

1 August 2017

Xiaoli Chen

6

1 reference

1 August 2017

Nahit M Mukaddes

7

1 reference

1 August 2017

Seung-Yun Yoo

8

1 reference

1 August 2017

Ellen Hanson

9

1 reference

1 August 2017

Rachel Hundley

10

1 reference

1 August 2017

Christina Austin

11

1 reference

1 August 2017

Ronald E Becker

12

1 reference

1 August 2017

Katherine Driscoll

14

1 reference

1 August 2017

Elizabeth C Engle

15

1 reference

1 August 2017

Sandra Friedman

16

1 reference

1 August 2017

Fuki M Hisama

18

1 reference

1 August 2017

Mira B Irons

19

1 reference

1 August 2017

Tina Lafiosca

20

1 reference

1 August 2017

Elaine LeClair

21

1 reference

1 August 2017

Michael Neessen

23

1 reference

1 August 2017

Jonathan D Picker

24

1 reference

1 August 2017

Cynthia M Rooney

26

1 reference

1 August 2017

Dean P Sarco

27

1 reference

1 August 2017

Joan M Stoler

28

1 reference

1 August 2017

Robert R Wolff

30

1 reference

1 August 2017

Ting Zhang

31

1 reference

1 August 2017

Ramzi H Nasir

32

1 reference

1 August 2017

Bai-Lin Wu

33

1 reference

1 August 2017

1 June 2010

1 reference

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

1 August 2017

1 reference

1 August 2017

153B

1 reference

1 August 2017

937-947

1 reference

1 August 2017

4

1 reference

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Common genetic variants on 5p14.1 associate with autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

A genome-wide investigation of SNPs and CNVs in schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Population analysis of large copy number variants and hotspots of human genetic disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Disruption of the neurexin 1 gene is associated with schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neuroligins and neurexins link synaptic function to cognitive disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Rare chromosomal deletions and duplications increase risk of schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Identifying autism loci and genes by tracing recent shared ancestry

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neurexin 1alpha structural variants associated with autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Significant association of the neurexin-1 gene (NRXN1) with nicotine dependence in European- and African-American smokers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Structural variation of chromosomes in autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Familial deletion within NLGN4 associated with autism and Tourette syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Disruption of neurexin 1 associated with autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Structural basis for synaptic adhesion mediated by neuroligin-neurexin interactions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Contribution of SHANK3 mutations to autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Synaptic arrangement of the neuroligin/beta-neurexin complex revealed by X-ray and neutron scattering

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Autism spectrum disorders: developmental disconnection syndromes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Novel genes identified in a high-density genome wide association study for nicotine dependence

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Important contribution of alpha-neurexins to Ca2+-triggered exocytosis of secretory granules.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Extracellular domains of alpha-neurexins participate in regulating synaptic transmission by selectively affecting N- and P/Q-type Ca2+ channels.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Postsynaptic assembly induced by neurexin-neuroligin interaction and neurotransmitter

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Is autism a disconnection disorder?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

The human genome browser at UCSC

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Structure and evolution of neurexin genes: insight into the mechanism of alternative splicing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Linkage and association of the glutamate receptor 6 gene with autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

A stoichiometric complex of neurexins and dystroglycan in brain

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Prediction of the coding sequences of unidentified human genes. IX. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neurexins: three genes and 1001 products

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Structures, alternative splicing, and neurexin binding of multiple neuroligins

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neuroligin 1: a splice site-specific ligand for beta-neurexins

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Deletion of alpha-neurexins does not cause a major impairment of axonal pathfinding or synapse formation.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

The expression and alternative splicing of alpha-neurexins during Xenopus development.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

White matter structure in autism: preliminary evidence from diffusion tensor imaging.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Cartography of neurexins: more than 1000 isoforms generated by alternative splicing and expressed in distinct subsets of neurons.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001124

Neurexins are differentially expressed in the embryonic nervous system of mice

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20468056

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.B.31063

1 reference

1 August 2017

1 reference

1 August 2017

1 reference